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Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing.
Rego, Shannon; Dagan-Rosenfeld, Orit; Bivona, Stephanie A; Snyder, Michael P; Ormond, Kelly E.
Afiliação
  • Rego S; Department of Genetics, Stanford University School of Medicine, Stanford, California.
  • Dagan-Rosenfeld O; Institute for Human Genetics, University of California-San Francisco, San Francisco, California.
  • Bivona SA; Department of Genetics, Stanford University School of Medicine, Stanford, California.
  • Snyder MP; Department of Genetics, Stanford University School of Medicine, Stanford, California.
  • Ormond KE; Department of Genetics, Stanford University School of Medicine, Stanford, California.
J Genet Couns ; 28(2): 428-437, 2019 04.
Article em En | MEDLINE | ID: mdl-30835913
The increasing availability of exome sequencing to the general ("healthy") population raises questions about the implications of genomic testing for individuals without suspected Mendelian diseases. Little is known about this population's motivations for undergoing exome sequencing, their expectations, reactions, and perceptions of utility. In order to address these questions, we conducted in-depth semi-structured interviews with 12 participants recruited from a longitudinal multi-omics profiling study that included exome sequencing. Participants were interviewed after receiving exome results, which included Mendelian disease-associated pathogenic and likely pathogenic variants, pharmacogenetic variants, and risk assessments for multifactorial diseases such as type 2 diabetes. The primary motivation driving participation in exome sequencing was personal curiosity. While they reported feeling validation and relief, participants were frequently underwhelmed by the results and described having expected more from exome sequencing. All participants reported discussing the results with at least some family, friends, and healthcare providers. Participants' recollection of the results returned to them was sometimes incorrect or incomplete, in many cases aligning with their perceptions of their health risks when entering the study. These results underscore the need for different genetic counseling approaches for generally healthy patients undergoing exome sequencing, in particular the need to provide anticipatory guidance to moderate participants' expectations. They also provide a preview of potential challenges clinicians may face as genomic sequencing continues to scale-up in the general population despite a lack of full understanding of its impact.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Sequenciamento do Exoma Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Sequenciamento do Exoma Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article